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Hannie Kremer PhD

+31 (0)24 361 04 87

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Hannie Kremer

Hannie Kremer's research focuses on hereditary deafness.

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Research group Usher syndrome: Genetics and functional genomics

Hannie Kremer's group aims to identify genetic defects that underlie hereditary hearing impairment and to unravel the molecular pathogenesis. Identification of deafness genes provides knowledge on inner ear function. Furthermore, it will provide handles for the development of future therapy.

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Field of study

Human genetics and otorhinolaryngology

Donders Institute for Brain, Cognition and Behaviour

The mission of the Donders Center for Medical Neuroscience is to carry out world class research that advances our knowledge on how the nervous system develops and functions and how it is altered by disease, injury, genetic, and environmental factors like stress.

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